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科學家發(fā)現(xiàn)亞洲人群或存在高頻率的EGFR突變率
時間:2014-02-18 14:01:45 來源:轉(zhuǎn)化醫(yī)學網(wǎng) 點擊:

長期以來,腺癌組織學、雌性、不吸煙狀態(tài)以及亞洲族群被認為是和非小細胞肺癌患者EGFR(表皮生長因子受體)突變相關的重要因子;近日,一項刊登在國際雜志Journal of Thoracic Oncology上的研究報告中,來自中國北京癌癥研究所的研究人員通過研究表明,在亞洲人群中EGFR突變的頻率相比之前報道的要高。




文章中,研究者表示,通過對亞洲7個區(qū)域大約1450位肺癌患者的研究發(fā)現(xiàn),在IIIB和IV期病人機體中EGFR突變的頻率為51.4%,而此前的報道大約為30%左右。




EGFR突變頻率在女性中為61.1%,在從不吸煙的個體中為60.7%;而EGFR突變頻率在男性中為44%,在偶然吸煙者機體中為51.6%;在亞洲區(qū)域中EGFR突變率最高的地區(qū)在越南,為64.2%,最低的區(qū)域在印度,為22.2%。




研究者Yuankai Shi博士表示,通過進行人口統(tǒng)計以及在臨床亞群上對EGFR突變頻率的研究揭示,EGFR突變的檢測應當在處于IIIB和IV期的肺癌亞洲病人中進行,這對于幫助病人及時改善治療策略以及確定其最佳的療法非常關鍵。


原文鏈接:





A Prospective, Molecular Epidemiology Study of EGFR Mutations in Asian Patients with Advanced Non–Small-Cell Lung Cancer of Adenocarcinoma Histology (PIONEER)




Shi, Yuankai MD*; Au, Joseph Siu-Kie MD†; Thongprasert, Sumitra MD‡; Srinivasan, Sankar MBBS§; Tsai, Chun-Ming MD‖; Khoa, Mai Trong MD¶; Heeroma, Karin Dr Med Sc#; Itoh, Yohji PhD**; Cornelio, Gerardo MD††; Yang, Pan-Chyr MD‡‡


Introduction: PIONEER (NCT01185314) was a prospective, multinational, epidemiological study of epidermal growth factor receptor (EGFR) mutations in patients from Asia with newly diagnosed advanced lung adenocarcinoma. Methods: Eligible patients (aged ≥20 years) had untreated stage IIIB/IV adenocarcinoma. The EGFR mutation status (primary end point: positive, negative, or undetermined) of tumor samples (biopsy, surgical specimen, or cytology) was determined (Scorpion amplification refractory mutation system). EGFR mutation frequency was calculated and compared between demographic and clinical subgroups. Results: Of 1482 patients from seven Asian regions, 43.4% of patients were female, median age was 60 years (range, 17–94), and 52.6% of patients were never-smokers. EGFR mutation status was evaluable in tumors from 1450 patients (97.8%) (746 [51.4%] positive; 704 [48.6%] negative). Country, sex, ethnicity, smoking status, pack-years (all p < 0.001), disease stage (p = 0.009), and histology type (p = 0.016) correlated significantly with EGFR mutation frequency. Mutation frequency was 61.1% in females, 44.0% in males; lower in patients from India (22.2%) compared with other areas (47.2%–64.2%); highest among never-smokers (60.7%); and decreased as pack-year number increased (>0–10 pack-years, 57.9%; >50 pack-years, 31.4%) (similar trend by sex). Ethnic group (p < 0.001) and pack-years (p < 0.001) had statistically significant associations with mutation frequency (multivariate analysis); sex was not significant when adjusted for smoking status. Conclusion: PIONEER is the first prospective study to confirm high EGFR mutation frequency (51.4% overall) in tumors from Asian patients with adenocarcinoma. The observed high mutation frequency in demographic/clinical subgroups compared with white populations suggests that mutation testing should be considered for all patients with stage IIIB/IV adenocarcinoma, even males and regular smokers, among Asian populations.

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